Canonical Allele Identifier: CA7691437

Gene: FAH

Linked Data

• ClinVar Variation Id: 1153592
• ClinVar RCV Id: RCV001495301 ; RCV003966011
• dbSNP Id: rs373285527
• ExAC: 15:80472513 C / T
• gnomAD v2: 15-80472513-C-T
• gnomAD v3: 15-80180171-C-T
• gnomAD v4: 15-80180171-C-T
• COSMIC: COSM2011622
• MyVariant Identifiers: chr15:g.80472513C>T (hg19) ; chr15:g.80180171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180171C>T , CM000677.2:g.80180171C>T	GRCh38
NC_000015.9:g.80472513C>T , CM000677.1:g.80472513C>T	GRCh37
NC_000015.8:g.78259568C>T	NCBI36
NG_012833.1:g.32173C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1097C>T
ENST00000561421.6:c.1008C>T MANE Select	ENSP00000453347.2:p.Asn336=
ENST00000646551.1:n.2622C>T
ENST00000261755.9:c.1008C>T	ENSP00000261755.5:p.Asn336=
ENST00000407106.5:c.1008C>T	ENSP00000385080.1:p.Asn336=
ENST00000539156.5:c.798C>T	ENSP00000454271.1:p.Asn266=
ENST00000559217.1:n.225C>T
ENST00000561353.2:c.106C>T
ENST00000561421.5:c.1008C>T	ENSP00000453347.1:p.Asn336=
NM_000137.2:c.1008C>T	NP_000128.1:p.Asn336=
XM_024449872.1:c.1008C>T	XP_024305640.1:p.Asn336=
NM_000137.4:c.1008C>T MANE Select	NP_000128.1:p.Asn336=
NM_001374377.1:c.1008C>T	NP_001361306.1:p.Asn336=
NM_001374380.1:c.1008C>T	NP_001361309.1:p.Asn336=